Working for The Royal Marsden

Join our world-class team and you will be part of a centre of excellence with an international reputation and a commitment to developing your career

Please wait, loading


NHS AfC: Band 6/7

Main area
NHS AfC: Band 6/7
Fixed term - 2 years
Full Time 37.5 hours per week
Job ref
Royal Marsden NHS Foundation Trust
Employer type
The Royal Marsden, Sutton
Sutton, Greater London
£34,961 - £48,515 pa inc hcas
21/05/2019 23:59

Royal Marsden Statisticians / Senior Statisticians (Band 6 / 7)

An exciting opportunity has arisen for statisticians / senior statistician (band 6/7) to join the Royal Marsden Clinical Trials Unit (RM CTU) which supports the Royal Marsden’s large, varied and innovative portfolio of studies ranging from early to late phase trials, and from simple to complex interventions.
The Royal Marsden is a world leader in cancer research, treatment and education. Together with our academic partner, The Institute of Cancer Research (ICR), we are the largest comprehensive cancer centre in Europe and the only National Institute of Health Research (NIHR) Biomedical Research Centre (BRC) specialising in cancer in the UK.
The RM CTU is currently employing a team of 9 statisticians and wishes to expand its statistical team further following our full accreditation from the UK Clinical Research Collaboration (UKCRC) Registered Clinical Trials Units Network. RM CTU supports the Research Themes of the only cancer specific Biomedical Research Centre (BRC).
We are looking for enthusiastic and self-motivated team members to contribute to the statistical and methodological considerations in study design and analysis of cancer clinical trials and studies. We are offering flexible working hours, excellent NHS pension and many opportunities for training and career development.

• The statistician/ senior statistician (band 6/7) will provide support and advice relating to statistical and analytical aspects for all Royal Marsden clinical trials working actively as a trial team member along with clinicians, trial managers and database programmers.
• A post-graduate qualification in medical statistics is required.
• Experience in STATA, and/or SAS/ SPSS is essential and experience in clinical trial data management systems would be desirable.
• For the senior role extensive experience in clinical trials is essential and familiarity with the regulatory environment surrounding clinical trials is desirable.

You should also have:
• A flexible but organized approach to work with the ability to work under pressure and to meet tight deadlines.
• The ability to work independently, as well as part of a small multi-disciplinary trial team and with colleagues across more than clinical unit.
• Strong written and verbal communication skills. 
• For the senior/lead roles experience in line management is desirable.

No smoking policyStonewall equality policy. Equality and justice for lesbians, gay men, bisexual and trans people.Disability confident employerCare quality commission - Outstanding

Documents to download

To print a document or save it to your computer, please click with your right mouse button on the document title and select "Save Target As...". You can then save the document in a suitable place on your computer ready to print it out. Clicking with the left mouse button will open the document in a new window (if your web browser can do so).

Apply online now

Further details / informal visits contact

Clare Peckitt ( / 0208 915 6269)

If you have problems applying, contact

Recruitment Support Team
01629 690825